首页> 外文期刊>Biology of Reproduction: Offical Journal of the Society for the Study of Reproduction >Early growth response gene-1 regulates the expression of the rat luteinizing hormone receptor gene.
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Early growth response gene-1 regulates the expression of the rat luteinizing hormone receptor gene.

机译:早期生长反应基因-1调节大鼠促黄体生成激素受体基因的表达。

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摘要

LH receptor gene expression is primarily regulated via specific interactions of trans-acting proteins and cis-acting DNA sequences in the upstream region of the gene. In this study, we report, using luciferase assays, that the region between -171 and -137 base pairs (bp) is essential for basal expression of the rat LH receptor gene. To identify factors that interact with the region between -171 and -137 bp and regulate expression of the gene, a rat granulosa cell cDNA library was screened using a yeast one-hybrid system. A positive clone, isolated by the screening, encodes a transcription factor early growth response gene-1 (Egr-1). To determine the sequence to which Egr-1 protein binds, electrophoretic mobility shift assay (EMSA) was employed. The Egr-1 protein was produced by an in vitro transcription/translation system using a full-length rat Egr-1 cDNA. The upstream region between -171 and -137 bp contains 2 overlapping Egr-1 consensus sequences. The EMSA revealed that Egr-1 binds independently to both sites. The overexpression of Egr-1 in MA-10 cells caused an approximately 2-fold increase in reporter luciferase activity. However, no induction of the luciferase activity was observed when luciferase constructs that lacked or had mutations in either or both of the Egr-1 sites were used, indicating that Egr-1 positively regulates LH receptor gene expression. In differentiated granulosa cells that had been pretreated with FSH for 48 h, the levels of both mRNA and Egr-1 protein were induced by hCG or cAMP, reaching maximal levels approximately 1.5 h after treatment and then returning to basal levels 8 h thereafter. No Egr-1 mRNA or protein was detected in undifferentiated granulosa cells, even after stimulation with 8-bromoadenosine-cAMP. These results suggest that Egr-1 functions only in luteinized granulosa cells after stimulation with hCG or cAMP. In conclusion, the findings demonstrate that Egr-1 actually binds to the regulatory upstream region of the LH receptor gene and positively regulates receptor gene expression. In addition, Egr-1 expression was observed only in luteinized granulosa cells after stimulation with hCG or cAMP. The present study provides further support to the hypothesis that Egr-1 plays important roles in the pituitary-gonadal axis.
机译:LH受体基因的表达主要通过基因上游区域中反式作用蛋白与顺式作用DNA序列的特异性相互作用来调节。在这项研究中,我们报告使用荧光素酶测定法,在-171和-137个碱基对(bp)之间的区域对于大鼠LH受体基因的基础表达至关重要。为了鉴定与-171和-137 bp之间的区域相互作用并调节该基因表达的因子,使用酵母单杂交系统筛选了大鼠颗粒细胞的cDNA文库。通过筛选分离出的阳性克隆编码转录因子早期生长反应基因1(Egr-1)。为了确定Egr-1蛋白结合的序列,采用了电泳迁移率变动分析(EMSA)。 Egr-1蛋白是通过使用全长大鼠Egr-1 cDNA的体外转录/翻译系统产生的。 -171和-137 bp之间的上游区域包含2个重叠的Egr-1共有序列。 EMSA显示,Egr-1独立结合到两个位点。 MA-10细胞中Egr-1的过度表达导致报告荧光素酶活性增加了约2倍。然而,当使用在两个或两个Egr-1位点中缺少或具有突变的荧光素酶构建体时,未观察到荧光素酶活性的诱导,表明Egr-1正调控LH受体基因的表达。在已经用FSH预处理48小时的分化颗粒细胞中,hCG或cAMP诱导mRNA和Egr-1蛋白的水平,在处理后约1.5 h达到最大水平,然后在8 h后恢复到基础水平。即使在用8-溴腺苷-cAMP刺激后,未分化的颗粒细胞中也未检测到Egr-1 mRNA或蛋白质。这些结果表明,在用hCG或cAMP刺激后,Egr-1仅在黄素化的颗粒细胞中起作用。总之,这些发现表明,Egr-1实际上与LH受体基因的上游调节区域结合,并正向调节受体基因的表达。另外,仅在用hCG或cAMP刺激后在黄素化的颗粒细胞中观察到Egr-1表达。本研究为Egr-1在垂体-性腺轴中起重要作用的假设提供了进一步的支持。

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